W WCG IRB Trademark

Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the human subjects of research; providing regulatory compliance consultation services in the nature of advice concerning due diligence, strategic development, and regulatory policy in the field of clinical trials involving human subjects; providing information relating to regulatory compliance for independent review of clinical trials involving human subjects

Non-downloadable software for use by clinical researchers, research sponsors and clinical research organizations for use in automating the submission, review and approval process of human subject clinical research projects